[{"publication_status":"published","date_updated":"2025-11-10T09:17:59Z","intvolume":"        10","title":"Organocatalyzed Synthesis of Oleochemical Carbonates from CO<sub>2</sub>and Renewables","year":"2017","author":[{"first_name":"Hendrik","last_name":"Büttner","full_name":"Büttner, Hendrik"},{"last_name":"Steinbauer","first_name":"Johannes","full_name":"Steinbauer, Johannes"},{"full_name":"Wulf, Christoph","last_name":"Wulf","first_name":"Christoph"},{"full_name":"Dindaroglu, Mehmet","first_name":"Mehmet","last_name":"Dindaroglu"},{"full_name":"Schmalz, Hans-Günther","first_name":"Hans-Günther","last_name":"Schmalz"},{"id":"89271","full_name":"Werner, Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","first_name":"Thomas"}],"publication_identifier":{"issn":["1864-5631"]},"doi":"10.1002/cssc.201601163","language":[{"iso":"eng"}],"extern":"1","publication":"ChemSusChem","issue":"6","type":"journal_article","keyword":["T1","T2","CSSD"],"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"date_created":"2023-01-22T21:00:17Z","status":"public","user_id":"89271","volume":10,"page":"1076-1079","_id":"37978","publisher":"Wiley","citation":{"ieee":"H. Büttner, J. Steinbauer, C. Wulf, M. Dindaroglu, H.-G. Schmalz, and T. Werner, “Organocatalyzed Synthesis of Oleochemical Carbonates from CO<sub>2</sub>and Renewables,” <i>ChemSusChem</i>, vol. 10, no. 6, pp. 1076–1079, 2017, doi: <a href=\"https://doi.org/10.1002/cssc.201601163\">10.1002/cssc.201601163</a>.","apa":"Büttner, H., Steinbauer, J., Wulf, C., Dindaroglu, M., Schmalz, H.-G., &#38; Werner, T. (2017). Organocatalyzed Synthesis of Oleochemical Carbonates from CO<sub>2</sub>and Renewables. <i>ChemSusChem</i>, <i>10</i>(6), 1076–1079. <a href=\"https://doi.org/10.1002/cssc.201601163\">https://doi.org/10.1002/cssc.201601163</a>","chicago":"Büttner, Hendrik, Johannes Steinbauer, Christoph Wulf, Mehmet Dindaroglu, Hans-Günther Schmalz, and Thomas Werner. “Organocatalyzed Synthesis of Oleochemical Carbonates from CO<sub>2</sub>and Renewables.” <i>ChemSusChem</i> 10, no. 6 (2017): 1076–79. <a href=\"https://doi.org/10.1002/cssc.201601163\">https://doi.org/10.1002/cssc.201601163</a>.","short":"H. Büttner, J. Steinbauer, C. Wulf, M. Dindaroglu, H.-G. Schmalz, T. Werner, ChemSusChem 10 (2017) 1076–1079.","mla":"Büttner, Hendrik, et al. “Organocatalyzed Synthesis of Oleochemical Carbonates from CO<sub>2</sub>and Renewables.” <i>ChemSusChem</i>, vol. 10, no. 6, Wiley, 2017, pp. 1076–79, doi:<a href=\"https://doi.org/10.1002/cssc.201601163\">10.1002/cssc.201601163</a>.","bibtex":"@article{Büttner_Steinbauer_Wulf_Dindaroglu_Schmalz_Werner_2017, title={Organocatalyzed Synthesis of Oleochemical Carbonates from CO<sub>2</sub>and Renewables}, volume={10}, DOI={<a href=\"https://doi.org/10.1002/cssc.201601163\">10.1002/cssc.201601163</a>}, number={6}, journal={ChemSusChem}, publisher={Wiley}, author={Büttner, Hendrik and Steinbauer, Johannes and Wulf, Christoph and Dindaroglu, Mehmet and Schmalz, Hans-Günther and Werner, Thomas}, year={2017}, pages={1076–1079} }","ama":"Büttner H, Steinbauer J, Wulf C, Dindaroglu M, Schmalz H-G, Werner T. Organocatalyzed Synthesis of Oleochemical Carbonates from CO<sub>2</sub>and Renewables. <i>ChemSusChem</i>. 2017;10(6):1076-1079. doi:<a href=\"https://doi.org/10.1002/cssc.201601163\">10.1002/cssc.201601163</a>"}},{"citation":{"chicago":"Schirmer, Marie-Luis, Stefan Jopp, Jens Holz, Anke Spannenberg, and Thomas Werner. “Organocatalyzed Reduction of Tertiary Phosphine Oxides.” <i>Advanced Synthesis and Catalysis</i> 358, no. 1 (2016): 26–29. <a href=\"https://doi.org/10.1002/adsc.201500762\">https://doi.org/10.1002/adsc.201500762</a>.","short":"M.-L. Schirmer, S. Jopp, J. Holz, A. Spannenberg, T. Werner, Advanced Synthesis and Catalysis 358 (2016) 26–29.","ieee":"M.-L. Schirmer, S. Jopp, J. Holz, A. Spannenberg, and T. Werner, “Organocatalyzed Reduction of Tertiary Phosphine Oxides,” <i>Advanced Synthesis and Catalysis</i>, vol. 358, no. 1, pp. 26–29, 2016, doi: <a href=\"https://doi.org/10.1002/adsc.201500762\">10.1002/adsc.201500762</a>.","apa":"Schirmer, M.-L., Jopp, S., Holz, J., Spannenberg, A., &#38; Werner, T. (2016). Organocatalyzed Reduction of Tertiary Phosphine Oxides. <i>Advanced Synthesis and Catalysis</i>, <i>358</i>(1), 26–29. <a href=\"https://doi.org/10.1002/adsc.201500762\">https://doi.org/10.1002/adsc.201500762</a>","bibtex":"@article{Schirmer_Jopp_Holz_Spannenberg_Werner_2016, title={Organocatalyzed Reduction of Tertiary Phosphine Oxides}, volume={358}, DOI={<a href=\"https://doi.org/10.1002/adsc.201500762\">10.1002/adsc.201500762</a>}, number={1}, journal={Advanced Synthesis and Catalysis}, publisher={Wiley}, author={Schirmer, Marie-Luis and Jopp, Stefan and Holz, Jens and Spannenberg, Anke and Werner, Thomas}, year={2016}, pages={26–29} }","ama":"Schirmer M-L, Jopp S, Holz J, Spannenberg A, Werner T. Organocatalyzed Reduction of Tertiary Phosphine Oxides. <i>Advanced Synthesis and Catalysis</i>. 2016;358(1):26-29. doi:<a href=\"https://doi.org/10.1002/adsc.201500762\">10.1002/adsc.201500762</a>","mla":"Schirmer, Marie-Luis, et al. “Organocatalyzed Reduction of Tertiary Phosphine Oxides.” <i>Advanced Synthesis and Catalysis</i>, vol. 358, no. 1, Wiley, 2016, pp. 26–29, doi:<a href=\"https://doi.org/10.1002/adsc.201500762\">10.1002/adsc.201500762</a>."},"publisher":"Wiley","_id":"37989","page":"26-29","volume":358,"user_id":"89271","status":"public","date_created":"2023-01-22T21:05:14Z","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T2","CSSD"],"type":"journal_article","publication":"Advanced Synthesis and Catalysis","issue":"1","extern":"1","language":[{"iso":"eng"}],"doi":"10.1002/adsc.201500762","publication_identifier":{"issn":["1615-4150"]},"author":[{"first_name":"Marie-Luis","last_name":"Schirmer","full_name":"Schirmer, Marie-Luis"},{"first_name":"Stefan","last_name":"Jopp","full_name":"Jopp, Stefan"},{"full_name":"Holz, Jens","first_name":"Jens","last_name":"Holz"},{"full_name":"Spannenberg, Anke","last_name":"Spannenberg","first_name":"Anke"},{"full_name":"Werner, Thomas","last_name":"Werner","first_name":"Thomas","orcid":"0000-0001-9025-3244","id":"89271"}],"year":"2016","title":"Organocatalyzed Reduction of Tertiary Phosphine Oxides","intvolume":"       358","publication_status":"published","date_updated":"2025-11-10T09:22:07Z"},{"citation":{"apa":"Schirmer, M.-L., Spannenberg, A., &#38; Werner, T. (2016). Highly functionalized alkenes produced from base-free organocatalytic Wittig reactions: (<i>E</i>)-3-benzylidenepyrrolidine-2,5-dione, (<i>E</i>)-3-benzylidene-1-methylpyrrolidine-2,5-dione and (<i>E</i>)-3-benzylidene-1-<i>tert</i>-butylpyrrolidine-2,5-dione. <i>Acta Crystallographica Section C Structural Chemistry</i>, <i>72</i>(6), 504–508. <a href=\"https://doi.org/10.1107/s2053229616008159\">https://doi.org/10.1107/s2053229616008159</a>","ieee":"M.-L. Schirmer, A. Spannenberg, and T. Werner, “Highly functionalized alkenes produced from base-free organocatalytic Wittig reactions: (<i>E</i>)-3-benzylidenepyrrolidine-2,5-dione, (<i>E</i>)-3-benzylidene-1-methylpyrrolidine-2,5-dione and (<i>E</i>)-3-benzylidene-1-<i>tert</i>-butylpyrrolidine-2,5-dione,” <i>Acta Crystallographica Section C Structural Chemistry</i>, vol. 72, no. 6, pp. 504–508, 2016, doi: <a href=\"https://doi.org/10.1107/s2053229616008159\">10.1107/s2053229616008159</a>.","short":"M.-L. Schirmer, A. Spannenberg, T. Werner, Acta Crystallographica Section C Structural Chemistry 72 (2016) 504–508.","chicago":"Schirmer, Marie-Luis, Anke Spannenberg, and Thomas Werner. “Highly Functionalized Alkenes Produced from Base-Free Organocatalytic Wittig Reactions: (<i>E</i>)-3-Benzylidenepyrrolidine-2,5-Dione, (<i>E</i>)-3-Benzylidene-1-Methylpyrrolidine-2,5-Dione and (<i>E</i>)-3-Benzylidene-1-<i>Tert</i>-Butylpyrrolidine-2,5-Dione.” <i>Acta Crystallographica Section C Structural Chemistry</i> 72, no. 6 (2016): 504–8. <a href=\"https://doi.org/10.1107/s2053229616008159\">https://doi.org/10.1107/s2053229616008159</a>.","mla":"Schirmer, Marie-Luis, et al. “Highly Functionalized Alkenes Produced from Base-Free Organocatalytic Wittig Reactions: (<i>E</i>)-3-Benzylidenepyrrolidine-2,5-Dione, (<i>E</i>)-3-Benzylidene-1-Methylpyrrolidine-2,5-Dione and (<i>E</i>)-3-Benzylidene-1-<i>Tert</i>-Butylpyrrolidine-2,5-Dione.” <i>Acta Crystallographica Section C Structural Chemistry</i>, vol. 72, no. 6, International Union of Crystallography (IUCr), 2016, pp. 504–08, doi:<a href=\"https://doi.org/10.1107/s2053229616008159\">10.1107/s2053229616008159</a>.","ama":"Schirmer M-L, Spannenberg A, Werner T. Highly functionalized alkenes produced from base-free organocatalytic Wittig reactions: (<i>E</i>)-3-benzylidenepyrrolidine-2,5-dione, (<i>E</i>)-3-benzylidene-1-methylpyrrolidine-2,5-dione and (<i>E</i>)-3-benzylidene-1-<i>tert</i>-butylpyrrolidine-2,5-dione. <i>Acta Crystallographica Section C Structural Chemistry</i>. 2016;72(6):504-508. doi:<a href=\"https://doi.org/10.1107/s2053229616008159\">10.1107/s2053229616008159</a>","bibtex":"@article{Schirmer_Spannenberg_Werner_2016, title={Highly functionalized alkenes produced from base-free organocatalytic Wittig reactions: (<i>E</i>)-3-benzylidenepyrrolidine-2,5-dione, (<i>E</i>)-3-benzylidene-1-methylpyrrolidine-2,5-dione and (<i>E</i>)-3-benzylidene-1-<i>tert</i>-butylpyrrolidine-2,5-dione}, volume={72}, DOI={<a href=\"https://doi.org/10.1107/s2053229616008159\">10.1107/s2053229616008159</a>}, number={6}, journal={Acta Crystallographica Section C Structural Chemistry}, publisher={International Union of Crystallography (IUCr)}, author={Schirmer, Marie-Luis and Spannenberg, Anke and Werner, Thomas}, year={2016}, pages={504–508} }"},"_id":"37984","publisher":"International Union of Crystallography (IUCr)","page":"504-508","volume":72,"user_id":"89271","status":"public","date_created":"2023-01-22T21:03:23Z","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T2"],"type":"journal_article","issue":"6","publication":"Acta Crystallographica Section C Structural Chemistry","extern":"1","abstract":[{"lang":"eng","text":"<jats:p>The Wittig reaction is a fundamental transformation for the preparation of alkenes from carbonyl compounds and phosphonium ylides. The ylides are prepared prior to the olefination step from the respective phosphonium salts by deprotonation utilizing strong bases. A first free-base catalytic Wittig reaction for the preparation of highly functionalized alkenes was based on tributylphosphane as the catalyst. Subsequently we developed a system employing a phospholene oxide as a pre-catalyst and trimethoxysilane as reducing agent which operates under milder conditions. The title compounds, (<jats:italic>E</jats:italic>)-3-benzylidenepyrrolidine-2,5-dione, C<jats:sub>11</jats:sub>H<jats:sub>9</jats:sub>NO<jats:sub>2</jats:sub>, (I), the methylpyrrolidine derivative, C<jats:sub>12</jats:sub>H<jats:sub>11</jats:sub>NO<jats:sub>2</jats:sub>, (II), and the<jats:italic>tert-</jats:italic>butylpyrrolidine derivative, C<jats:sub>15</jats:sub>H<jats:sub>17</jats:sub>NO<jats:sub>2</jats:sub>, (III), have been synthesized by base-free catalytic Wittig reactions. In the crystal of (I), molecules are linked into centrosymmetric dimers<jats:italic>via</jats:italic>pairs of N—H...O hydrogen bonds. Furthermore, in the crystal structure of (III), there are two molecules in the asymmetric unit, whereas in (I) and (II), only one molecule is present.</jats:p>"}],"language":[{"iso":"eng"}],"doi":"10.1107/s2053229616008159","author":[{"last_name":"Schirmer","first_name":"Marie-Luis","full_name":"Schirmer, Marie-Luis"},{"last_name":"Spannenberg","first_name":"Anke","full_name":"Spannenberg, Anke"},{"orcid":"0000-0001-9025-3244","first_name":"Thomas","last_name":"Werner","full_name":"Werner, Thomas","id":"89271"}],"publication_identifier":{"issn":["2053-2296"]},"year":"2016","title":"Highly functionalized alkenes produced from base-free organocatalytic Wittig reactions: (<i>E</i>)-3-benzylidenepyrrolidine-2,5-dione, (<i>E</i>)-3-benzylidene-1-methylpyrrolidine-2,5-dione and (<i>E</i>)-3-benzylidene-1-<i>tert</i>-butylpyrrolidine-2,5-dione","intvolume":"        72","publication_status":"published","date_updated":"2025-11-10T09:23:46Z"},{"citation":{"bibtex":"@article{Schirmer_Adomeit_Spannenberg_Werner_2016, title={Novel Base-Free Catalytic Wittig Reaction for the Synthesis of Highly Functionalized Alkenes}, volume={22}, DOI={<a href=\"https://doi.org/10.1002/chem.201503744\">10.1002/chem.201503744</a>}, number={7}, journal={Chemistry - A European Journal}, publisher={Wiley}, author={Schirmer, Marie-Luis and Adomeit, Sven and Spannenberg, Anke and Werner, Thomas}, year={2016}, pages={2458–2465} }","ama":"Schirmer M-L, Adomeit S, Spannenberg A, Werner T. Novel Base-Free Catalytic Wittig Reaction for the Synthesis of Highly Functionalized Alkenes. <i>Chemistry - A European Journal</i>. 2016;22(7):2458-2465. doi:<a href=\"https://doi.org/10.1002/chem.201503744\">10.1002/chem.201503744</a>","mla":"Schirmer, Marie-Luis, et al. “Novel Base-Free Catalytic Wittig Reaction for the Synthesis of Highly Functionalized Alkenes.” <i>Chemistry - A European Journal</i>, vol. 22, no. 7, Wiley, 2016, pp. 2458–65, doi:<a href=\"https://doi.org/10.1002/chem.201503744\">10.1002/chem.201503744</a>.","short":"M.-L. Schirmer, S. Adomeit, A. Spannenberg, T. Werner, Chemistry - A European Journal 22 (2016) 2458–2465.","chicago":"Schirmer, Marie-Luis, Sven Adomeit, Anke Spannenberg, and Thomas Werner. “Novel Base-Free Catalytic Wittig Reaction for the Synthesis of Highly Functionalized Alkenes.” <i>Chemistry - A European Journal</i> 22, no. 7 (2016): 2458–65. <a href=\"https://doi.org/10.1002/chem.201503744\">https://doi.org/10.1002/chem.201503744</a>.","ieee":"M.-L. Schirmer, S. Adomeit, A. Spannenberg, and T. Werner, “Novel Base-Free Catalytic Wittig Reaction for the Synthesis of Highly Functionalized Alkenes,” <i>Chemistry - A European Journal</i>, vol. 22, no. 7, pp. 2458–2465, 2016, doi: <a href=\"https://doi.org/10.1002/chem.201503744\">10.1002/chem.201503744</a>.","apa":"Schirmer, M.-L., Adomeit, S., Spannenberg, A., &#38; Werner, T. (2016). Novel Base-Free Catalytic Wittig Reaction for the Synthesis of Highly Functionalized Alkenes. <i>Chemistry - A European Journal</i>, <i>22</i>(7), 2458–2465. <a href=\"https://doi.org/10.1002/chem.201503744\">https://doi.org/10.1002/chem.201503744</a>"},"status":"public","volume":22,"user_id":"89271","_id":"37986","publisher":"Wiley","page":"2458-2465","extern":"1","issue":"7","publication":"Chemistry - A European Journal","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T2","CSSD"],"type":"journal_article","date_created":"2023-01-22T21:04:06Z","intvolume":"        22","date_updated":"2025-11-10T09:23:00Z","publication_status":"published","author":[{"last_name":"Schirmer","first_name":"Marie-Luis","full_name":"Schirmer, Marie-Luis"},{"first_name":"Sven","last_name":"Adomeit","full_name":"Adomeit, Sven"},{"first_name":"Anke","last_name":"Spannenberg","full_name":"Spannenberg, Anke"},{"id":"89271","first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","full_name":"Werner, Thomas"}],"publication_identifier":{"issn":["0947-6539"]},"title":"Novel Base-Free Catalytic Wittig Reaction for the Synthesis of Highly Functionalized Alkenes","year":"2016","doi":"10.1002/chem.201503744","language":[{"iso":"eng"}]},{"title":"Phospholane-Catalyzed Wittig Reaction","year":"2015","publication_identifier":{"issn":["1434-193X"]},"author":[{"full_name":"Werner, Thomas","first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","id":"89271"},{"first_name":"Marcel","last_name":"Hoffmann","full_name":"Hoffmann, Marcel"},{"last_name":"Deshmukh","first_name":"Sunetra","full_name":"Deshmukh, Sunetra"}],"date_updated":"2025-11-10T09:27:56Z","publication_status":"published","intvolume":"      2015","language":[{"iso":"eng"}],"doi":"10.1002/ejoc.201500243","alternative_title":["Phospholane-Catalyzed Wittig Reaction"],"issue":"15","publication":"European Journal of Organic Chemistry","extern":"1","date_created":"2023-01-22T21:07:48Z","keyword":["T2","CSSD"],"type":"journal_article","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"status":"public","page":"3286-3295","_id":"37996","publisher":"Wiley","user_id":"89271","volume":2015,"citation":{"ieee":"T. Werner, M. Hoffmann, and S. Deshmukh, “Phospholane-Catalyzed Wittig Reaction,” <i>European Journal of Organic Chemistry</i>, vol. 2015, no. 15, pp. 3286–3295, 2015, doi: <a href=\"https://doi.org/10.1002/ejoc.201500243\">10.1002/ejoc.201500243</a>.","apa":"Werner, T., Hoffmann, M., &#38; Deshmukh, S. (2015). Phospholane-Catalyzed Wittig Reaction. <i>European Journal of Organic Chemistry</i>, <i>2015</i>(15), 3286–3295. <a href=\"https://doi.org/10.1002/ejoc.201500243\">https://doi.org/10.1002/ejoc.201500243</a>","chicago":"Werner, Thomas, Marcel Hoffmann, and Sunetra Deshmukh. “Phospholane-Catalyzed Wittig Reaction.” <i>European Journal of Organic Chemistry</i> 2015, no. 15 (2015): 3286–95. <a href=\"https://doi.org/10.1002/ejoc.201500243\">https://doi.org/10.1002/ejoc.201500243</a>.","short":"T. Werner, M. Hoffmann, S. Deshmukh, European Journal of Organic Chemistry 2015 (2015) 3286–3295.","mla":"Werner, Thomas, et al. “Phospholane-Catalyzed Wittig Reaction.” <i>European Journal of Organic Chemistry</i>, vol. 2015, no. 15, Wiley, 2015, pp. 3286–95, doi:<a href=\"https://doi.org/10.1002/ejoc.201500243\">10.1002/ejoc.201500243</a>.","bibtex":"@article{Werner_Hoffmann_Deshmukh_2015, title={Phospholane-Catalyzed Wittig Reaction}, volume={2015}, DOI={<a href=\"https://doi.org/10.1002/ejoc.201500243\">10.1002/ejoc.201500243</a>}, number={15}, journal={European Journal of Organic Chemistry}, publisher={Wiley}, author={Werner, Thomas and Hoffmann, Marcel and Deshmukh, Sunetra}, year={2015}, pages={3286–3295} }","ama":"Werner T, Hoffmann M, Deshmukh S. Phospholane-Catalyzed Wittig Reaction. <i>European Journal of Organic Chemistry</i>. 2015;2015(15):3286-3295. doi:<a href=\"https://doi.org/10.1002/ejoc.201500243\">10.1002/ejoc.201500243</a>"}},{"status":"public","volume":71,"user_id":"89271","publisher":"International Union of Crystallography (IUCr)","_id":"37991","page":"o872-o872","citation":{"short":"M.-L. Schirmer, A. Spannenberg, T. Werner, Acta Crystallographica Section E Crystallographic Communications 71 (2015) o872–o872.","chicago":"Schirmer, Marie-Luis, Anke Spannenberg, and Thomas Werner. “Crystal Structure of Diethyl (<i>E</i>)-2-[(Benzofuran-2-Yl)Methylidene]Succinate.” <i>Acta Crystallographica Section E Crystallographic Communications</i> 71, no. 11 (2015): o872–o872. <a href=\"https://doi.org/10.1107/s2056989015019313\">https://doi.org/10.1107/s2056989015019313</a>.","ieee":"M.-L. Schirmer, A. Spannenberg, and T. Werner, “Crystal structure of diethyl (<i>E</i>)-2-[(benzofuran-2-yl)methylidene]succinate,” <i>Acta Crystallographica Section E Crystallographic Communications</i>, vol. 71, no. 11, pp. o872–o872, 2015, doi: <a href=\"https://doi.org/10.1107/s2056989015019313\">10.1107/s2056989015019313</a>.","apa":"Schirmer, M.-L., Spannenberg, A., &#38; Werner, T. (2015). Crystal structure of diethyl (<i>E</i>)-2-[(benzofuran-2-yl)methylidene]succinate. <i>Acta Crystallographica Section E Crystallographic Communications</i>, <i>71</i>(11), o872–o872. <a href=\"https://doi.org/10.1107/s2056989015019313\">https://doi.org/10.1107/s2056989015019313</a>","bibtex":"@article{Schirmer_Spannenberg_Werner_2015, title={Crystal structure of diethyl (<i>E</i>)-2-[(benzofuran-2-yl)methylidene]succinate}, volume={71}, DOI={<a href=\"https://doi.org/10.1107/s2056989015019313\">10.1107/s2056989015019313</a>}, number={11}, journal={Acta Crystallographica Section E Crystallographic Communications}, publisher={International Union of Crystallography (IUCr)}, author={Schirmer, Marie-Luis and Spannenberg, Anke and Werner, Thomas}, year={2015}, pages={o872–o872} }","ama":"Schirmer M-L, Spannenberg A, Werner T. Crystal structure of diethyl (<i>E</i>)-2-[(benzofuran-2-yl)methylidene]succinate. <i>Acta Crystallographica Section E Crystallographic Communications</i>. 2015;71(11):o872-o872. doi:<a href=\"https://doi.org/10.1107/s2056989015019313\">10.1107/s2056989015019313</a>","mla":"Schirmer, Marie-Luis, et al. “Crystal Structure of Diethyl (<i>E</i>)-2-[(Benzofuran-2-Yl)Methylidene]Succinate.” <i>Acta Crystallographica Section E Crystallographic Communications</i>, vol. 71, no. 11, International Union of Crystallography (IUCr), 2015, pp. o872–o872, doi:<a href=\"https://doi.org/10.1107/s2056989015019313\">10.1107/s2056989015019313</a>."},"intvolume":"        71","publication_status":"published","date_updated":"2025-11-10T09:28:18Z","author":[{"first_name":"Marie-Luis","last_name":"Schirmer","full_name":"Schirmer, Marie-Luis"},{"full_name":"Spannenberg, Anke","first_name":"Anke","last_name":"Spannenberg"},{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271"}],"publication_identifier":{"issn":["2056-9890"]},"year":"2015","title":"Crystal structure of diethyl (<i>E</i>)-2-[(benzofuran-2-yl)methylidene]succinate","doi":"10.1107/s2056989015019313","language":[{"iso":"eng"}],"extern":"1","abstract":[{"text":"<jats:p>The title compound, C<jats:sub>17</jats:sub>H<jats:sub>18</jats:sub>O<jats:sub>5</jats:sub>, was synthesized by a base-free catalytic Wittig reaction. The molecule consists of a diethyl itaconate unit, which is connected<jats:italic>via</jats:italic>the C=C double bond to a benzofuran moiety. The benzofuran ring system (r.m.s. deviation = 0.007 Å) forms dihedral angles of 79.58 (4) and 12.12 (10)° with the mean planes through the<jats:italic>cis</jats:italic>and<jats:italic>trans</jats:italic>ethoxycarbonyl groups, respectively. An intramolecular C—H...O hydrogen bond involving the O atom of the benzofuran moiety is observed. In the crystal, molecules are linked into ribbons running parallel to the<jats:italic>b</jats:italic>axis by C—H...O hydrogen bonds.</jats:p>","lang":"eng"}],"publication":"Acta Crystallographica Section E Crystallographic Communications","issue":"11","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T2"],"type":"journal_article","date_created":"2023-01-22T21:06:01Z"},{"intvolume":"      2015","publication_status":"published","date_updated":"2025-11-10T09:29:30Z","author":[{"full_name":"Hoffmann, Marcel","first_name":"Marcel","last_name":"Hoffmann"},{"first_name":"Sunetra","last_name":"Deshmukh","full_name":"Deshmukh, Sunetra"},{"id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"}],"publication_identifier":{"issn":["1434-193X"]},"year":"2015","title":"Scope and Limitation of the Microwave-Assisted Catalytic Wittig Reaction","alternative_title":["The Microwave-Assisted Catalytic Wittig Reaction"],"doi":"10.1002/ejoc.201500310","language":[{"iso":"eng"}],"extern":"1","issue":"20","publication":"European Journal of Organic Chemistry","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T2","CSSD"],"type":"journal_article","date_created":"2023-01-22T21:07:09Z","status":"public","volume":2015,"user_id":"89271","_id":"37994","publisher":"Wiley","page":"4532-4543","citation":{"mla":"Hoffmann, Marcel, et al. “Scope and Limitation of the Microwave-Assisted Catalytic Wittig Reaction.” <i>European Journal of Organic Chemistry</i>, vol. 2015, no. 20, Wiley, 2015, pp. 4532–43, doi:<a href=\"https://doi.org/10.1002/ejoc.201500310\">10.1002/ejoc.201500310</a>.","ama":"Hoffmann M, Deshmukh S, Werner T. Scope and Limitation of the Microwave-Assisted Catalytic Wittig Reaction. <i>European Journal of Organic Chemistry</i>. 2015;2015(20):4532-4543. doi:<a href=\"https://doi.org/10.1002/ejoc.201500310\">10.1002/ejoc.201500310</a>","bibtex":"@article{Hoffmann_Deshmukh_Werner_2015, title={Scope and Limitation of the Microwave-Assisted Catalytic Wittig Reaction}, volume={2015}, DOI={<a href=\"https://doi.org/10.1002/ejoc.201500310\">10.1002/ejoc.201500310</a>}, number={20}, journal={European Journal of Organic Chemistry}, publisher={Wiley}, author={Hoffmann, Marcel and Deshmukh, Sunetra and Werner, Thomas}, year={2015}, pages={4532–4543} }","apa":"Hoffmann, M., Deshmukh, S., &#38; Werner, T. (2015). Scope and Limitation of the Microwave-Assisted Catalytic Wittig Reaction. <i>European Journal of Organic Chemistry</i>, <i>2015</i>(20), 4532–4543. <a href=\"https://doi.org/10.1002/ejoc.201500310\">https://doi.org/10.1002/ejoc.201500310</a>","ieee":"M. Hoffmann, S. Deshmukh, and T. Werner, “Scope and Limitation of the Microwave-Assisted Catalytic Wittig Reaction,” <i>European Journal of Organic Chemistry</i>, vol. 2015, no. 20, pp. 4532–4543, 2015, doi: <a href=\"https://doi.org/10.1002/ejoc.201500310\">10.1002/ejoc.201500310</a>.","chicago":"Hoffmann, Marcel, Sunetra Deshmukh, and Thomas Werner. “Scope and Limitation of the Microwave-Assisted Catalytic Wittig Reaction.” <i>European Journal of Organic Chemistry</i> 2015, no. 20 (2015): 4532–43. <a href=\"https://doi.org/10.1002/ejoc.201500310\">https://doi.org/10.1002/ejoc.201500310</a>.","short":"M. Hoffmann, S. Deshmukh, T. Werner, European Journal of Organic Chemistry 2015 (2015) 4532–4543."}},{"extern":"1","issue":"11","publication":"ACS Sustainable Chemistry and Engineering","keyword":["T1","T2","CSSD"],"type":"journal_article","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"date_created":"2023-01-22T21:06:26Z","publication_status":"published","date_updated":"2025-11-10T09:30:37Z","intvolume":"         3","title":"Recycling of Phosphorus-Based Organocatalysts by Organic Solvent Nanofiltration","year":"2015","author":[{"full_name":"Großeheilmann, Julia","last_name":"Großeheilmann","first_name":"Julia"},{"full_name":"Büttner, Hendrik","last_name":"Büttner","first_name":"Hendrik"},{"full_name":"Kohrt, Christina","first_name":"Christina","last_name":"Kohrt"},{"full_name":"Kragl, Udo","last_name":"Kragl","first_name":"Udo"},{"id":"89271","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas","full_name":"Werner, Thomas"}],"publication_identifier":{"issn":["2168-0485","2168-0485"]},"doi":"10.1021/acssuschemeng.5b00734","language":[{"iso":"eng"}],"citation":{"bibtex":"@article{Großeheilmann_Büttner_Kohrt_Kragl_Werner_2015, title={Recycling of Phosphorus-Based Organocatalysts by Organic Solvent Nanofiltration}, volume={3}, DOI={<a href=\"https://doi.org/10.1021/acssuschemeng.5b00734\">10.1021/acssuschemeng.5b00734</a>}, number={11}, journal={ACS Sustainable Chemistry and Engineering}, publisher={American Chemical Society (ACS)}, author={Großeheilmann, Julia and Büttner, Hendrik and Kohrt, Christina and Kragl, Udo and Werner, Thomas}, year={2015}, pages={2817–2822} }","ama":"Großeheilmann J, Büttner H, Kohrt C, Kragl U, Werner T. Recycling of Phosphorus-Based Organocatalysts by Organic Solvent Nanofiltration. <i>ACS Sustainable Chemistry and Engineering</i>. 2015;3(11):2817-2822. doi:<a href=\"https://doi.org/10.1021/acssuschemeng.5b00734\">10.1021/acssuschemeng.5b00734</a>","mla":"Großeheilmann, Julia, et al. “Recycling of Phosphorus-Based Organocatalysts by Organic Solvent Nanofiltration.” <i>ACS Sustainable Chemistry and Engineering</i>, vol. 3, no. 11, American Chemical Society (ACS), 2015, pp. 2817–22, doi:<a href=\"https://doi.org/10.1021/acssuschemeng.5b00734\">10.1021/acssuschemeng.5b00734</a>.","chicago":"Großeheilmann, Julia, Hendrik Büttner, Christina Kohrt, Udo Kragl, and Thomas Werner. “Recycling of Phosphorus-Based Organocatalysts by Organic Solvent Nanofiltration.” <i>ACS Sustainable Chemistry and Engineering</i> 3, no. 11 (2015): 2817–22. <a href=\"https://doi.org/10.1021/acssuschemeng.5b00734\">https://doi.org/10.1021/acssuschemeng.5b00734</a>.","short":"J. Großeheilmann, H. Büttner, C. Kohrt, U. Kragl, T. Werner, ACS Sustainable Chemistry and Engineering 3 (2015) 2817–2822.","ieee":"J. Großeheilmann, H. Büttner, C. Kohrt, U. Kragl, and T. Werner, “Recycling of Phosphorus-Based Organocatalysts by Organic Solvent Nanofiltration,” <i>ACS Sustainable Chemistry and Engineering</i>, vol. 3, no. 11, pp. 2817–2822, 2015, doi: <a href=\"https://doi.org/10.1021/acssuschemeng.5b00734\">10.1021/acssuschemeng.5b00734</a>.","apa":"Großeheilmann, J., Büttner, H., Kohrt, C., Kragl, U., &#38; Werner, T. (2015). Recycling of Phosphorus-Based Organocatalysts by Organic Solvent Nanofiltration. <i>ACS Sustainable Chemistry and Engineering</i>, <i>3</i>(11), 2817–2822. <a href=\"https://doi.org/10.1021/acssuschemeng.5b00734\">https://doi.org/10.1021/acssuschemeng.5b00734</a>"},"status":"public","user_id":"89271","volume":3,"page":"2817-2822","_id":"37992","publisher":"American Chemical Society (ACS)"},{"intvolume":"         8","publication_status":"published","date_updated":"2025-11-10T09:31:34Z","author":[{"first_name":"Hendrik","last_name":"Büttner","full_name":"Büttner, Hendrik"},{"first_name":"Johannes","last_name":"Steinbauer","full_name":"Steinbauer, Johannes"},{"id":"89271","first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas"}],"publication_identifier":{"issn":["1864-5631"]},"year":"2015","title":"Synthesis of Cyclic Carbonates from Epoxides and Carbon Dioxide by Using Bifunctional One-Component Phosphorus-Based Organocatalysts","doi":"10.1002/cssc.201500612","language":[{"iso":"eng"}],"extern":"1","issue":"16","publication":"ChemSusChem","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T1","T2","CSSD"],"type":"journal_article","date_created":"2023-01-22T21:06:51Z","status":"public","volume":8,"user_id":"89271","_id":"37993","publisher":"Wiley","page":"2655-2669","citation":{"apa":"Büttner, H., Steinbauer, J., &#38; Werner, T. (2015). Synthesis of Cyclic Carbonates from Epoxides and Carbon Dioxide by Using Bifunctional One-Component Phosphorus-Based Organocatalysts. <i>ChemSusChem</i>, <i>8</i>(16), 2655–2669. <a href=\"https://doi.org/10.1002/cssc.201500612\">https://doi.org/10.1002/cssc.201500612</a>","ieee":"H. Büttner, J. Steinbauer, and T. Werner, “Synthesis of Cyclic Carbonates from Epoxides and Carbon Dioxide by Using Bifunctional One-Component Phosphorus-Based Organocatalysts,” <i>ChemSusChem</i>, vol. 8, no. 16, pp. 2655–2669, 2015, doi: <a href=\"https://doi.org/10.1002/cssc.201500612\">10.1002/cssc.201500612</a>.","chicago":"Büttner, Hendrik, Johannes Steinbauer, and Thomas Werner. “Synthesis of Cyclic Carbonates from Epoxides and Carbon Dioxide by Using Bifunctional One-Component Phosphorus-Based Organocatalysts.” <i>ChemSusChem</i> 8, no. 16 (2015): 2655–69. <a href=\"https://doi.org/10.1002/cssc.201500612\">https://doi.org/10.1002/cssc.201500612</a>.","short":"H. Büttner, J. Steinbauer, T. Werner, ChemSusChem 8 (2015) 2655–2669.","mla":"Büttner, Hendrik, et al. “Synthesis of Cyclic Carbonates from Epoxides and Carbon Dioxide by Using Bifunctional One-Component Phosphorus-Based Organocatalysts.” <i>ChemSusChem</i>, vol. 8, no. 16, Wiley, 2015, pp. 2655–69, doi:<a href=\"https://doi.org/10.1002/cssc.201500612\">10.1002/cssc.201500612</a>.","ama":"Büttner H, Steinbauer J, Werner T. Synthesis of Cyclic Carbonates from Epoxides and Carbon Dioxide by Using Bifunctional One-Component Phosphorus-Based Organocatalysts. <i>ChemSusChem</i>. 2015;8(16):2655-2669. doi:<a href=\"https://doi.org/10.1002/cssc.201500612\">10.1002/cssc.201500612</a>","bibtex":"@article{Büttner_Steinbauer_Werner_2015, title={Synthesis of Cyclic Carbonates from Epoxides and Carbon Dioxide by Using Bifunctional One-Component Phosphorus-Based Organocatalysts}, volume={8}, DOI={<a href=\"https://doi.org/10.1002/cssc.201500612\">10.1002/cssc.201500612</a>}, number={16}, journal={ChemSusChem}, publisher={Wiley}, author={Büttner, Hendrik and Steinbauer, Johannes and Werner, Thomas}, year={2015}, pages={2655–2669} }"}},{"citation":{"short":"C. Kohrt, T. Werner, ChemSusChem 8 (2015) 2031–2034.","chicago":"Kohrt, Christina, and Thomas Werner. “Recyclable Bifunctional Polystyrene and Silica Gel-Supported Organocatalyst for the Coupling of CO<sub>2</sub>with Epoxides.” <i>ChemSusChem</i> 8, no. 12 (2015): 2031–34. <a href=\"https://doi.org/10.1002/cssc.201500128\">https://doi.org/10.1002/cssc.201500128</a>.","apa":"Kohrt, C., &#38; Werner, T. (2015). Recyclable Bifunctional Polystyrene and Silica Gel-Supported Organocatalyst for the Coupling of CO<sub>2</sub>with Epoxides. <i>ChemSusChem</i>, <i>8</i>(12), 2031–2034. <a href=\"https://doi.org/10.1002/cssc.201500128\">https://doi.org/10.1002/cssc.201500128</a>","ieee":"C. Kohrt and T. Werner, “Recyclable Bifunctional Polystyrene and Silica Gel-Supported Organocatalyst for the Coupling of CO<sub>2</sub>with Epoxides,” <i>ChemSusChem</i>, vol. 8, no. 12, pp. 2031–2034, 2015, doi: <a href=\"https://doi.org/10.1002/cssc.201500128\">10.1002/cssc.201500128</a>.","ama":"Kohrt C, Werner T. Recyclable Bifunctional Polystyrene and Silica Gel-Supported Organocatalyst for the Coupling of CO<sub>2</sub>with Epoxides. <i>ChemSusChem</i>. 2015;8(12):2031-2034. doi:<a href=\"https://doi.org/10.1002/cssc.201500128\">10.1002/cssc.201500128</a>","bibtex":"@article{Kohrt_Werner_2015, title={Recyclable Bifunctional Polystyrene and Silica Gel-Supported Organocatalyst for the Coupling of CO<sub>2</sub>with Epoxides}, volume={8}, DOI={<a href=\"https://doi.org/10.1002/cssc.201500128\">10.1002/cssc.201500128</a>}, number={12}, journal={ChemSusChem}, publisher={Wiley}, author={Kohrt, Christina and Werner, Thomas}, year={2015}, pages={2031–2034} }","mla":"Kohrt, Christina, and Thomas Werner. “Recyclable Bifunctional Polystyrene and Silica Gel-Supported Organocatalyst for the Coupling of CO<sub>2</sub>with Epoxides.” <i>ChemSusChem</i>, vol. 8, no. 12, Wiley, 2015, pp. 2031–34, doi:<a href=\"https://doi.org/10.1002/cssc.201500128\">10.1002/cssc.201500128</a>."},"status":"public","page":"2031-2034","_id":"37997","publisher":"Wiley","user_id":"89271","volume":8,"issue":"12","publication":"ChemSusChem","extern":"1","date_created":"2023-01-22T21:08:10Z","type":"journal_article","keyword":["T1","T2","CSSD"],"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"year":"2015","title":"Recyclable Bifunctional Polystyrene and Silica Gel-Supported Organocatalyst for the Coupling of CO<sub>2</sub>with Epoxides","publication_identifier":{"issn":["1864-5631"]},"author":[{"full_name":"Kohrt, Christina","first_name":"Christina","last_name":"Kohrt"},{"full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","first_name":"Thomas","last_name":"Werner","id":"89271"}],"publication_status":"published","date_updated":"2025-11-10T09:30:13Z","intvolume":"         8","language":[{"iso":"eng"}],"doi":"10.1002/cssc.201500128"},{"citation":{"ieee":"W. Desens, C. Kohrt, M. Frank, and T. Werner, “Highly Efficient Polymer-Supported Catalytic System for the Valorization of Carbon Dioxide,” <i>ChemSusChem</i>, vol. 8, no. 22, pp. 3815–3822, 2015, doi: <a href=\"https://doi.org/10.1002/cssc.201501119\">10.1002/cssc.201501119</a>.","apa":"Desens, W., Kohrt, C., Frank, M., &#38; Werner, T. (2015). Highly Efficient Polymer-Supported Catalytic System for the Valorization of Carbon Dioxide. <i>ChemSusChem</i>, <i>8</i>(22), 3815–3822. <a href=\"https://doi.org/10.1002/cssc.201501119\">https://doi.org/10.1002/cssc.201501119</a>","chicago":"Desens, Willi, Christina Kohrt, Marcus Frank, and Thomas Werner. “Highly Efficient Polymer-Supported Catalytic System for the Valorization of Carbon Dioxide.” <i>ChemSusChem</i> 8, no. 22 (2015): 3815–22. <a href=\"https://doi.org/10.1002/cssc.201501119\">https://doi.org/10.1002/cssc.201501119</a>.","short":"W. Desens, C. Kohrt, M. Frank, T. Werner, ChemSusChem 8 (2015) 3815–3822.","mla":"Desens, Willi, et al. “Highly Efficient Polymer-Supported Catalytic System for the Valorization of Carbon Dioxide.” <i>ChemSusChem</i>, vol. 8, no. 22, Wiley, 2015, pp. 3815–22, doi:<a href=\"https://doi.org/10.1002/cssc.201501119\">10.1002/cssc.201501119</a>.","bibtex":"@article{Desens_Kohrt_Frank_Werner_2015, title={Highly Efficient Polymer-Supported Catalytic System for the Valorization of Carbon Dioxide}, volume={8}, DOI={<a href=\"https://doi.org/10.1002/cssc.201501119\">10.1002/cssc.201501119</a>}, number={22}, journal={ChemSusChem}, publisher={Wiley}, author={Desens, Willi and Kohrt, Christina and Frank, Marcus and Werner, Thomas}, year={2015}, pages={3815–3822} }","ama":"Desens W, Kohrt C, Frank M, Werner T. Highly Efficient Polymer-Supported Catalytic System for the Valorization of Carbon Dioxide. <i>ChemSusChem</i>. 2015;8(22):3815-3822. doi:<a href=\"https://doi.org/10.1002/cssc.201501119\">10.1002/cssc.201501119</a>"},"volume":8,"user_id":"89271","publisher":"Wiley","_id":"37990","page":"3815-3822","status":"public","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T1","T2","CSSD"],"type":"journal_article","date_created":"2023-01-22T21:05:43Z","extern":"1","publication":"ChemSusChem","issue":"22","doi":"10.1002/cssc.201501119","language":[{"iso":"eng"}],"intvolume":"         8","date_updated":"2025-11-10T09:31:09Z","publication_status":"published","publication_identifier":{"issn":["1864-5631"]},"author":[{"full_name":"Desens, Willi","last_name":"Desens","first_name":"Willi"},{"first_name":"Christina","last_name":"Kohrt","full_name":"Kohrt, Christina"},{"first_name":"Marcus","last_name":"Frank","full_name":"Frank, Marcus"},{"id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","first_name":"Thomas","last_name":"Werner"}],"title":"Highly Efficient Polymer-Supported Catalytic System for the Valorization of Carbon Dioxide","year":"2015"},{"language":[{"iso":"eng"}],"doi":"10.1021/acs.orglett.5b01352","publication_identifier":{"issn":["1523-7060","1523-7052"]},"author":[{"full_name":"Schirmer, Marie-Luis","last_name":"Schirmer","first_name":"Marie-Luis"},{"full_name":"Adomeit, Sven","first_name":"Sven","last_name":"Adomeit"},{"full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas","id":"89271"}],"year":"2015","title":"First Base-Free Catalytic Wittig Reaction","intvolume":"        17","publication_status":"published","date_updated":"2025-11-10T09:28:45Z","date_created":"2023-01-22T21:07:30Z","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["T2","CSSD"],"issue":"12","publication":"Organic Letters","extern":"1","_id":"37995","publisher":"American Chemical Society (ACS)","page":"3078-3081","volume":17,"user_id":"89271","status":"public","citation":{"chicago":"Schirmer, Marie-Luis, Sven Adomeit, and Thomas Werner. “First Base-Free Catalytic Wittig Reaction.” <i>Organic Letters</i> 17, no. 12 (2015): 3078–81. <a href=\"https://doi.org/10.1021/acs.orglett.5b01352\">https://doi.org/10.1021/acs.orglett.5b01352</a>.","short":"M.-L. Schirmer, S. Adomeit, T. Werner, Organic Letters 17 (2015) 3078–3081.","ama":"Schirmer M-L, Adomeit S, Werner T. First Base-Free Catalytic Wittig Reaction. <i>Organic Letters</i>. 2015;17(12):3078-3081. doi:<a href=\"https://doi.org/10.1021/acs.orglett.5b01352\">10.1021/acs.orglett.5b01352</a>","bibtex":"@article{Schirmer_Adomeit_Werner_2015, title={First Base-Free Catalytic Wittig Reaction}, volume={17}, DOI={<a href=\"https://doi.org/10.1021/acs.orglett.5b01352\">10.1021/acs.orglett.5b01352</a>}, number={12}, journal={Organic Letters}, publisher={American Chemical Society (ACS)}, author={Schirmer, Marie-Luis and Adomeit, Sven and Werner, Thomas}, year={2015}, pages={3078–3081} }","apa":"Schirmer, M.-L., Adomeit, S., &#38; Werner, T. (2015). First Base-Free Catalytic Wittig Reaction. <i>Organic Letters</i>, <i>17</i>(12), 3078–3081. <a href=\"https://doi.org/10.1021/acs.orglett.5b01352\">https://doi.org/10.1021/acs.orglett.5b01352</a>","mla":"Schirmer, Marie-Luis, et al. “First Base-Free Catalytic Wittig Reaction.” <i>Organic Letters</i>, vol. 17, no. 12, American Chemical Society (ACS), 2015, pp. 3078–81, doi:<a href=\"https://doi.org/10.1021/acs.orglett.5b01352\">10.1021/acs.orglett.5b01352</a>.","ieee":"M.-L. Schirmer, S. Adomeit, and T. Werner, “First Base-Free Catalytic Wittig Reaction,” <i>Organic Letters</i>, vol. 17, no. 12, pp. 3078–3081, 2015, doi: <a href=\"https://doi.org/10.1021/acs.orglett.5b01352\">10.1021/acs.orglett.5b01352</a>."}},{"citation":{"apa":"Werner, T., Hoffmann, M., &#38; Deshmukh, S. (2014). First Microwave-Assisted Catalytic Wittig Reaction. <i>European Journal of Organic Chemistry</i>, <i>2014</i>(31), 6873–6876. <a href=\"https://doi.org/10.1002/ejoc.201403113\">https://doi.org/10.1002/ejoc.201403113</a>","ieee":"T. Werner, M. Hoffmann, and S. Deshmukh, “First Microwave-Assisted Catalytic Wittig Reaction,” <i>European Journal of Organic Chemistry</i>, vol. 2014, no. 31, pp. 6873–6876, 2014, doi: <a href=\"https://doi.org/10.1002/ejoc.201403113\">10.1002/ejoc.201403113</a>.","short":"T. Werner, M. Hoffmann, S. 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